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FDA 510(k)

COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE

K-Number: K933456 · 1993-11-02

ApplicantConmedcorp
Decision Date1993-11-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K933456. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE?

COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Conmedcorp. The 510(k) number is K933456.

When did COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE receive FDA 510(k) clearance?

COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE received FDA 510(k) clearance on 1993-11-02, under 510(k) number K933456.

Who is the listed applicant for COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE?

The FDA 510(k) record lists Conmedcorp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE?

The FDA product code for COMED TROGARD(TM) BLUNT TIP TROCAR/SLEEVE is GCJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Conmedcorp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 92 devices →

Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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